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HRID 526作成日:2026年10月24日

Tert-butyl cis-(3-carbamoylcyclohexyl)carbamate → tert-butyl N-[(1R,3S)-3-[[4-(6,6-dimethyl-5,7-dihydropyrrolo[1,2-a]imidazol-3-yl)-5-fluoro-2-pyridinyl]carbamoyl]cyclohexyl]carbamate

https://huagongshe.com/ja/reaction/526

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl cis-(3-carbamoylcyclohexyl)carbamateHCID 71279992—
反応物3-(2-Chloro-5-fluoro-4-pyridinyl)-6,6-dimethyl-5,7-dihydropyrrolo[1,2-a]imidazoleHCID 124155277—
試薬Cesium carbonateHCID 10796—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒1,4-DioxaneHCID 31275—
生成物tert-butyl N-[(1R,3S)-3-[[4-(6,6-dimethyl-5,7-dihydropyrrolo[1,2-a]imidazol-3-yl)-5-fluoro-2-pyridinyl]carbamoyl]cyclohexyl]carbamateHCID 12416404880.01%

反応条件

温度120 °C

反応手順

Tetrakis(triphenylphosphine)palladium(0) (43.5 mg, 0.04 mmol) was added to 3-(2-chloro-5-fluoropyridin-4-yl)-6,6-dimethyl-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole (100 mg, 0.38 mmol), tert-butyl ((1R,3S)-3-carbamoylcyclohexyl)carbamate (109 mg, 0.45 mmol) and 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (43.6 mg, 0.08 mmol) and Cesium carbonate (368 mg, 1.13 mmol) in 1,4-dioxane (5.98 ml). Degassed for 5 mins under nitrogen and the resulting suspension was stirred at 120 °C for 3 hours in the microwave reactor. The reaction mixture was partitioned between water (20ml) and DCM (40ml) and separated using a phase separation cartridge. The organics were absorbed onto silica and purified by flash silica chromatography, elution gradient 0 to 60% EtOAc in heptane. Pure fractions were evaporated to dryness to afford starting material (100mg).

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-3648f11ef3b2438f8cb66069ce02004a
出典メモ750 AstraZeneca ELN dataset